DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM 9438-06 STT-MC-001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-05-09 for DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM 9438-06 STT-MC-001 manufactured by Dexcom, Inc..

Event Text Entries

[107854393] (b)(4). The patient experienced adverse events on different days with the same device. The following reports are being submitted. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[107854394] Dexcom was made aware on 04/10/2018, that on (b)(6) 2018, a loss of connection occurred. No data was provided for evaluation. Confirmation of the issue was undetermined. The probable cause could not be determined. No additional event or patient information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004753838-2018-049768
MDR Report Key7498683
Report SourceCONSUMER
Date Received2018-05-09
Date of Report2018-04-10
Date of Event2018-04-07
Date Mfgr Received2018-04-10
Device Manufacturer Date2017-12-29
Date Added to Maude2018-05-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR KIPP DURBIN
Manufacturer Street6340 SEQUENCE DR.
Manufacturer CitySAN DIEGO CA 92121
Manufacturer CountryUS
Manufacturer Postal92121
Manufacturer Phone8582000200
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
Generic NameCONTINUOUS GLUCOSE MONITOR
Product CodePDF
Date Received2018-05-09
Model Number9438-06
Catalog NumberSTT-MC-001
Lot Number6006178
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEXCOM, INC.
Manufacturer Address6340 SEQUENCE DR. SAN DIEGO CA 92121 US 92121


Patients

Patient NumberTreatmentOutcomeDate
10 2018-05-09

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.